Parental phonological memory contributes to prediction of outcome of late talkers from 20 months to 4 years: a longitudinal study of precursors of specific language impairment

Background

Many children who are late talkers go on to develop normal language, but others go on to have longer-term language difficulties. In this study, we considered which factors were predictive of persistent problems in late talkers.

Methods

Parental report of expressive vocabulary at 18 months of age was used to select 26 late talkers and 70 average talkers, who were assessed for language and cognitive ability at 20 months of age. Follow-up at 4 years of age was carried out for 24 late and 58 average talkers. A psychometric test battery was used to categorize children in terms of language status (unimpaired or impaired) and nonverbal ability (normal range or more than 1 SD below average). The vocabulary and non-word repetition skills of the accompanying parent were also assessed.

Results

Among the late talkers, seven (29%) met our criteria for specific language impairment (SLI) at 4 years of age, and a further two (8%) had low nonverbal ability. In the group of average talkers, eight (14%) met the criteria for SLI at 4 years, and five other children (8%) had low nonverbal ability. Family history of language problems was slightly better than late-talker status as a predictor of SLI.. The best predictors of SLI at 20 months of age were score on the receptive language scale of the Mullen Scales of Early Learning and the parent''s performance on a non-word repetition task. Maternal education was not a significant predictor of outcome.

Conclusions

In this study, around three-quarters of late talkers did not have any language difficulties at 4 years of age, provided there was no family history of language impairment. A family history of language-literacy problems was found to be a significant predictor for persisting problems. Nevertheless, there are children with SLI for whom prediction is difficult because they did not have early language delay.     

Novel mutations in the SH3BP2 gene associated with sporadic central giant cell lesions and cherubism

Central giant cell lesion (CGCL) is a reactive bone lesion that occurs mainly in the mandible, characterized by the multinucleated osteoclast-like giant cells in a background of oval to spindle-shaped mononuclear cells. The etiology is unknown and occurs more commonly in young adults. Cherubism, a rare disease found predominantly in females has histologic characteristics indistinguishable from those of CGCL and is caused by mutations mostly present in exon 9 of the SH3BP2 gene. In this study, we investigated four cases of CGCL and one case of cherubism. DNA was extracted from peripheral blood and tumor tissue and all coding and flanking regions of the SH3BP2 amplified by PCR and directly sequenced to identify underlying mutations. Two novel mutations were found; a heterozygous missense mutation c.1442A>T (Q481L) in exon 11 in one sporadic case of CGCL and a heterozygous germline and tumor tissue missense mutation c.320C>T (T107M) in exon 4 in one patient with cherubism. These findings open a new window to investigate the possible relationship between the pathogenesis of the cherubism and CGCL.     

Inflatable surface coil for MR imaging of the prostate

An inflatable surface coil for transrectal magnetic resonance imaging of the prostate was designed. The coil was tested during imaging of an insulated saline phantom and of the prostates of four patients. Phantom images were comparable to those obtained with commercial coils of similar size. High spatial resolution and excellent contrast were noted in coronal images of the prostates. Use of this coil could substantially improve studies of the prostate and cervix.     

The high signal intensity meniscus of the knee. Magnetic resonance evaluation and in vivo correlation

This study describes the different appearances of meniscal abnormalities on magnetic resonance (MR) images and correlates macroscopic and histologic findings. Twenty-three of 40 cadaveric menisci with MR signal abnormalities were examined macroscopically; five of the 23 were studied histologically. In addition, MR studies of seven patients (14 menisci) were examined and findings were correlated arthroscopically. Histologic analysis was performed on two of these menisci. The two major findings on MR images were: (1) abnormal, high, centrally located signal intensity within the meniscus and (2) disruption of the peripheral meniscal contour. Macroscopically evident meniscal degeneration correlated well with findings on MR images in all cases. Histologic abnormalities included microcyst formation and separation of collagen bundles. Four menisci with intact outer contour lines on MR images had macroscopically identifiable tears. In addition, two meniscal tears were appreciated only after intra-articular injection of gadolinium-DTPA. We conclude that MR imaging is superior to macroscopic examination as performed by arthroscopy or arthrotomy for the detection of degenerative meniscal lesions. The technique also accurately identifies meniscal tears, a capability that might be enhanced by prior intra-articular injection of MR contrast agents.     

Trigeminal nerve: anatomic correlation with MR imaging

Through correlation with cryomicrotic sections, the appearance of the trigeminal nerve and its branches on magnetic resonance images is described in healthy individuals and in patients with tumors involving this nerve. Coronal images are best for defining the different parts of the nerve and for making a side-to-side comparison. Sagittal images are useful to demonstrate tumors involving the gasserian ganglion.